{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dusseldorf",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83776",
      "recalling_firm": "Hager & Meisinger Gmbh",
      "address_1": "Ronsdorferstrasse 22",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: NV, PA, FL, SC, IA, NC-",
      "recall_number": "Z-0493-2020",
      "product_description": "Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end; US-No 245; Reference: HMUN245-009; Shank: FG/314; Head Size 1/10mm: 009,Head Length/mm:",
      "product_quantity": "2500 burs",
      "reason_for_recall": "Incorrect packaging; There is a potential that a  1.0 mm carbide blade was packaged  in a 0.9 mm carbide blade packaging.",
      "recall_initiation_date": "20181107",
      "center_classification_date": "20191119",
      "report_date": "20191127",
      "code_info": "Lot #R23891  UDI: +E0HM26UN2453140099/$$8250523R23891+"
    }
  ]
}